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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
retinitis pigmentosa +     
Aldred Syndrome 
Alstrom syndrome  
Amaurosis Hypertrichosis  
autosomal recessive pericentral pigmentary retinopathy 
Bork Stender Schmidt Syndrome 
Chang Davidson Carlson Syndrome 
Chromosome Xp11.3 Deletion Syndrome 
Concentric Annular Macular Dystrophy  
Cone Dystrophy 4  
Cone Rod Dystrophy Amelogenesis Imperfecta  
cone-rod dystrophy 1  
cone-rod dystrophy 10  
cone-rod dystrophy 11  
cone-rod dystrophy 13  
cone-rod dystrophy 14  
cone-rod dystrophy 16  
cone-rod dystrophy 17 
cone-rod dystrophy 19  
cone-rod dystrophy 2  
cone-rod dystrophy 20  
Cone-Rod Dystrophy 21  
cone-rod dystrophy 3  
cone-rod dystrophy 5  
cone-rod dystrophy 6  
cone-rod dystrophy 7  
cone-rod dystrophy 8 
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness  
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
dominant pericentral pigmentary retinopathy 
Flynn Aird Syndrome 
Furukawa Takagi Nakao Syndrome 
Hardikar Syndrome  
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA  
isolated microphthalmia 5  
Jalili syndrome  
Kearns-Sayre syndrome  
late-adult onset retinitis pigmentosa 
Leber congenital amaurosis 14  
Leber congenital amaurosis 3  
Macular Dystrophy with Central Cone Involvement  
Metaphyseal Chondrodysplasia with Retinitis Pigmentosa  
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract 
Mirhosseini-Holmes-Walton Syndrome 
multiple congenital anomalies-hypotonia-seizures syndrome 3  
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
NARP syndrome  
Newfoundland cone-rod dystrophy  
Oculotrichodysplasia 
Oliver-McFarlane syndrome  
Peripheral Cone Dystrophy 
PHARC syndrome  
Pigmentary Retinopathy and Sensorineural Deafness  
Posterior Column Ataxia with Retinitis Pigmentosa  
Progressive Pallidal Degeneration with Retinitis Pigmentosa 
Radioulnar Synostosis Retinal Pigment Abnormalities 
retinal cone dystrophy 3A  
retinal cone dystrophy 3B  
retinal cone dystrophy 4  
retinitis pigmentosa 1  
retinitis pigmentosa 10  
retinitis pigmentosa 11  
retinitis pigmentosa 12  
retinitis pigmentosa 13  
retinitis pigmentosa 14  
retinitis pigmentosa 17  
retinitis pigmentosa 18  
retinitis pigmentosa 19  
retinitis pigmentosa 2  
retinitis pigmentosa 20  
retinitis pigmentosa 22 
retinitis pigmentosa 23  
retinitis pigmentosa 24 
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retinitis pigmentosa 26  
retinitis pigmentosa 27  
retinitis pigmentosa 28  
retinitis pigmentosa 29 
retinitis pigmentosa 3  
retinitis pigmentosa 30  
retinitis pigmentosa 31  
retinitis pigmentosa 32  
retinitis pigmentosa 33  
retinitis pigmentosa 34 
retinitis pigmentosa 35  
retinitis pigmentosa 36  
retinitis pigmentosa 37  
retinitis pigmentosa 38  
retinitis pigmentosa 39  
retinitis pigmentosa 4  
retinitis pigmentosa 40  
retinitis pigmentosa 41  
retinitis pigmentosa 42  
retinitis pigmentosa 43  
retinitis pigmentosa 44  
retinitis pigmentosa 45  
retinitis pigmentosa 46  
retinitis pigmentosa 47  
retinitis pigmentosa 48  
retinitis pigmentosa 49  
retinitis pigmentosa 50  
retinitis pigmentosa 51  
A retinitis pigmentosa that has_material_basis_in mutation in the TTC8 gene on chromosome 14q31. (DO)
retinitis pigmentosa 54  
retinitis pigmentosa 55  
retinitis pigmentosa 56  
retinitis pigmentosa 57  
retinitis pigmentosa 58  
retinitis pigmentosa 59  
retinitis pigmentosa 6  
retinitis pigmentosa 60  
retinitis pigmentosa 61  
retinitis pigmentosa 62  
retinitis pigmentosa 63 
retinitis pigmentosa 66  
retinitis pigmentosa 67  
retinitis pigmentosa 68  
retinitis pigmentosa 69  
retinitis pigmentosa 7  
retinitis pigmentosa 70  
retinitis pigmentosa 71  
retinitis pigmentosa 72  
retinitis pigmentosa 73  
retinitis pigmentosa 74  
retinitis pigmentosa 75  
Retinitis Pigmentosa 76  
retinitis pigmentosa 77  
Retinitis Pigmentosa 78  
Retinitis Pigmentosa 79  
Retinitis Pigmentosa 80  
retinitis pigmentosa 81  
retinitis pigmentosa 83  
retinitis pigmentosa 84  
retinitis pigmentosa 85  
retinitis pigmentosa 86  
retinitis pigmentosa 87  
retinitis pigmentosa 88  
retinitis pigmentosa 89  
retinitis pigmentosa 9  
retinitis pigmentosa 90  
Retinitis Pigmentosa 92  
Retinitis Pigmentosa 93  
Retinitis Pigmentosa 95  
Retinitis Pigmentosa 96  
RETINITIS PIGMENTOSA 97  
RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS  
Retinitis Pigmentosa Inversa with Deafness 
retinitis pigmentosa with or without situs inversus  
Retinitis Pigmentosa with Paraarteriolar Preservation Of Retinal Pigment Epithelium 
retinitis pigmentosa Y-linked 
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 
Retinitis Pigmentosa, Late-Onset Dominant  
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa 
Rhizomelic Skeletal Dysplasia with Retinitis Pigmentosa 
RHYNS Syndrome  
Senior-Loken Syndrome 4  
Severe Mental Retardation, with Spasticity and Pigmentary Tapetoretinal Degeneration 
short stature, hearing loss, retinitis pigmentosa, and distinctive facies  
short-rib thoracic dysplasia 9 with or without polydactyly  
Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation 
spondylometaphyseal dysplasia with cone-rod dystrophy  
Tapetoretinal Degeneration with Ataxia 
Usher syndrome +   
X-Linked Cone Dystrophy with Tapetal-like Sheen 
X-linked cone-rod dystrophy 1  
X-linked cone-rod dystrophy 2 
X-linked cone-rod dystrophy 3  
X-linked retinitis pigmentosa and sinorespiratory infections  

Synonyms
Exact Synonyms: RP51
Broad Synonyms: TTC8-RELATED CONDITION
Primary IDs: OMIM:613464
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/20451172 "DO" "DO"

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